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Preparing a wedding....

Getting married in November. Feel like the stress of this won't help the ms... If anyone has any tips or owt on how to deal with it that'd be great, also ways on making it cheaper would be handy too 😂

@Comfortablynumb 

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Comfortablynumb

ANTIBIOTICS/ ANTIVIRALS as a first like of defence.

There are many studies out there looking for the catalyst for MS and quite a few points the finger at a Viral or Bacterial source. The obvious Viral one being Epstein Barr. Epstein Barr can cross the blood brain barrier and trick the immune system into attacking healthy cells studies show. Also, oth...

@shiftms-polls 

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shiftms-polls

Opinion check; Should HCPs discuss progression at diagnosis?

Are you the type of person who wants to know all of the facts about progression as early as possible, or would you rather cross that bridge when you get to it? There can be a lot of disparity surrounding the topic of progression, so let us know your thoughts down below 👇 Sharing your opinions c...

Should healthcare professionals discuss progression at diagnosis?

Total answers: 57

@Chooper 

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Chooper

London Marathon!!

Hi, calling all MSers!! My brother in law is running the London Marathon to raise money for the MS society because of my MS diagnosis. Amazingly the bank he works for is also match funding every donation which is brilliant! If anyone has a spare few pounds and wants to support him to help the MS Soc...

@DominicS 

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DominicS

Does Risk Management Matter Anymore?

An article I published on LinkedIn the other day: Or... Why Aren't MS Patients Worth It? Recently, I was sent a genetic test that won much acclaim at ECTRIMS 2023. The test is simple, fast, and unequivocal. Why is it important? As one of the 2.5 million plus Multiple Sclerosis (MS) patients in th...

Aubagio

Hello, everyone :) I'm currently on Rebif treatment. Got tired of the needles, so I asked my neurologist if there's any chance for me to change my therapy... She said that I could switch to Aubagio, but the things I've read about it are not that "jolly"... I was wondering if there's anyone here usin...

@Bigzbe34 

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Bigzbe34

One day post infusion

Slept so hard when I got home from my infusion. Took the day after off just in case I need more rest which I do but I’m looking forward to feeling better I’m thankful for this page and the people on it when I’m feeling depressed and alone it’s nice knowing I’m not alone. I am trying to feed the wolf...
Odessa, TX, USA

@KingCorbs24 

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KingCorbs24

Dating someone with MS.

Hello, I recently went on a date with a person who after the second date told me about their MS diagnosis. She is 36 and I'm 33. As soon as I found out I started doing my research. I've spent hours on Google and YouTube. Trying to learn as much as I can about it. My only experience previously wit...

@Msfighternadia 

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Msfighternadia

Hate my life

Suffering from depression due too ms. People are mean and dont understand what i go through, going on dates ends up being ignored, friends turning their backs on me and co worker thinking i am just using my ms as an excuse too not lift heavy😞

@shiftms-films 

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shiftms-films

Have you experienced loneliness because of your MS?

In this episode of MSers React Dave, Roxy, Katt and Heather respond to posts on Shift.ms about loneliness. Have you experienced loneliness because of your MS? If so you’re not alone! If you have an experience to share, or a way that you’ve learnt to adapt then please share your story in the comment...